Fetal lung C4BPA induces p100 processing in human placenta

Abstract The non-canonical NF-κB signaling may be a central integrator of a placental clock that governs the length of human pregnancy. We sought to identify fetal signals that could activate this NF-κB pathway in the placenta, and in turn, contribute to the onset of labor. Proteomics analysis of ex...

Full description

Bibliographic Details
Main Authors: Mayra Cruz Ithier, Nataliya Parobchak, Stacy Yadava, Jerry Cheng, Bingbing Wang, Todd Rosen
Format: Article
Language:English
Published: Nature Publishing Group 2019-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-019-42078-0
id doaj-ce25bda40c1c46b8a4cb3b799bb23b12
record_format Article
spelling doaj-ce25bda40c1c46b8a4cb3b799bb23b122020-12-08T06:35:06ZengNature Publishing GroupScientific Reports2045-23222019-04-019111010.1038/s41598-019-42078-0Fetal lung C4BPA induces p100 processing in human placentaMayra Cruz Ithier0Nataliya Parobchak1Stacy Yadava2Jerry Cheng3Bingbing Wang4Todd Rosen5Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical SchoolDepartment of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical SchoolDepartment of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical SchoolThe Cardiovascular Institute of New Jersey, Rutgers Robert Wood Johnson Medical SchoolDepartment of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical SchoolDepartment of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Rutgers Robert Wood Johnson Medical SchoolAbstract The non-canonical NF-κB signaling may be a central integrator of a placental clock that governs the length of human pregnancy. We sought to identify fetal signals that could activate this NF-κB pathway in the placenta, and in turn, contribute to the onset of labor. Proteomics analysis of exosomes purified from fetal cord arterial blood revealed a total of 328 proteins, among which 48 were more significantly abundant (p < 0.01) in samples from women who delivered following elective Cesarean-section at term (39 to 40 weeks of estimated gestational age, EGA) compared to those who had elective Cesarean deliveries near term (35 to 36 weeks of EGA). Computational, crystal structural, and gene functional analyses showed that one of these 48 proteins, C4BPA, binds to CD40 of placental villous trophoblast to activate p100 processing to p52, and in turn, pro-labor genes. These results suggest that fetal C4BPA-induced activation of non-canonical NF-κB in human placenta may play a critical role in processes of term or preterm labor.https://doi.org/10.1038/s41598-019-42078-0
collection DOAJ
language English
format Article
sources DOAJ
author Mayra Cruz Ithier
Nataliya Parobchak
Stacy Yadava
Jerry Cheng
Bingbing Wang
Todd Rosen
spellingShingle Mayra Cruz Ithier
Nataliya Parobchak
Stacy Yadava
Jerry Cheng
Bingbing Wang
Todd Rosen
Fetal lung C4BPA induces p100 processing in human placenta
Scientific Reports
author_facet Mayra Cruz Ithier
Nataliya Parobchak
Stacy Yadava
Jerry Cheng
Bingbing Wang
Todd Rosen
author_sort Mayra Cruz Ithier
title Fetal lung C4BPA induces p100 processing in human placenta
title_short Fetal lung C4BPA induces p100 processing in human placenta
title_full Fetal lung C4BPA induces p100 processing in human placenta
title_fullStr Fetal lung C4BPA induces p100 processing in human placenta
title_full_unstemmed Fetal lung C4BPA induces p100 processing in human placenta
title_sort fetal lung c4bpa induces p100 processing in human placenta
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2019-04-01
description Abstract The non-canonical NF-κB signaling may be a central integrator of a placental clock that governs the length of human pregnancy. We sought to identify fetal signals that could activate this NF-κB pathway in the placenta, and in turn, contribute to the onset of labor. Proteomics analysis of exosomes purified from fetal cord arterial blood revealed a total of 328 proteins, among which 48 were more significantly abundant (p < 0.01) in samples from women who delivered following elective Cesarean-section at term (39 to 40 weeks of estimated gestational age, EGA) compared to those who had elective Cesarean deliveries near term (35 to 36 weeks of EGA). Computational, crystal structural, and gene functional analyses showed that one of these 48 proteins, C4BPA, binds to CD40 of placental villous trophoblast to activate p100 processing to p52, and in turn, pro-labor genes. These results suggest that fetal C4BPA-induced activation of non-canonical NF-κB in human placenta may play a critical role in processes of term or preterm labor.
url https://doi.org/10.1038/s41598-019-42078-0
work_keys_str_mv AT mayracruzithier fetallungc4bpainducesp100processinginhumanplacenta
AT nataliyaparobchak fetallungc4bpainducesp100processinginhumanplacenta
AT stacyyadava fetallungc4bpainducesp100processinginhumanplacenta
AT jerrycheng fetallungc4bpainducesp100processinginhumanplacenta
AT bingbingwang fetallungc4bpainducesp100processinginhumanplacenta
AT toddrosen fetallungc4bpainducesp100processinginhumanplacenta
_version_ 1724391333364236288